@article{oai:kanazawa-u.repo.nii.ac.jp:00014920,
 author = {Somei, Masanori and Yamada, Yoshikazu and Kitagawa, Keiichi and Sugaya, Katsuko and Tomita, Yayoi and Yamada, Fumio and Nakagawa, Kyoko},
 issue = {3},
 journal = {Heterocycles},
 month = {Jan},
 note = {2-Amino-4-(1-methylindol-3-yl)thiazole (11c) has a characteristic nucleophilic nature at the 5-position and add to the 4-position of acetylpyridinium acetate (13) producing 2-acetylamino-5-(1-acetyl-1,4-dihydropyridin-4-yl)-4-(1-methylindol-3-yl) thiazole (1c). Its structure was established by X-ray single crystallographic analysis. Applying the results, simple syntheses of the related tris- (1a-b and 2-8) and tetrakis-linked heterocycles (9) were achieved., 金沢大学大学院自然科学研究科生理活性物質科学, 金沢大学薬学部},
 pages = {435--438},
 title = {Synthetic study directed toward novel multi-linked heterocycles},
 volume = {45},
 year = {1997}
}